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1 , and a significant proportion were terminal deoxynucleotidyl transferase (TdT) -mediated deoxyuridin
2 g (V[D]J) recombination, the enzyme terminal deoxynucleotidyl transferase (Tdt) adds random nucleotid
3 B cell progenitors fail to express terminal deoxynucleotidyl transferase (TdT) and for other reasons
5 rtoires due to the delayed onset of terminal deoxynucleotidyl transferase (TdT) expression in ontogen
6 hat mice expressing a transgene for terminal deoxynucleotidyl transferase (TdT) have nucleotide inser
7 mplate independent polymerases, and terminal deoxynucleotidyl transferase (TdT) in particular, have b
8 -OH of an RNA molecule, followed by terminal deoxynucleotidyl transferase (TdT) to catalyze the seque
9 6C(-) Thy-1(-)CD43(+) CD16/32(Lo/-) terminal deoxynucleotidyl transferase (TdT)(+) cells in murine bo
10 rrow (BM) chimeras, made with adult terminal deoxynucleotidyl transferase (TdT)(+/+) and TdT(-/-) don
12 le stranded DNA (ssDNA) chain using terminal deoxynucleotidyl transferase (TdT), a template-independe
14 ovium, we also sought expression of terminal deoxynucleotidyl transferase (TdT), which is normally ex
15 d (N) nucleotides is carried out by terminal deoxynucleotidyl transferase (TdT), whose only known phy
17 h HA were examined for apoptosis in terminal deoxynucleotidyl transferase (TdT)-mediated dUTP biotin
18 ive to WT animals, as documented by terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick en
19 y, we compared these tests with the terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick en
25 The short splice variant of mouse terminal deoxynucleotidyl transferase (TdTS) catalyzes the additi
26 ptase polymerase chain reaction and terminal deoxynucleotidyl transferase 2-deoxyuridine, 5-triphosph
32 Apoptotic cells were detected by terminal deoxynucleotidyl transferase catalyzed labeling of DNA f
33 s in the spleen, as measured by the terminal deoxynucleotidyl transferase deoxyuridine triphosphate n
35 hematoxylin and eosin staining, and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
36 f DNA-fragmentation was detected by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
37 rations >1% (v/v), using annexin V, terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
38 mmunosorbent assays and in liver by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
40 cells did not stain positively for terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
41 illibrand factor (vWF) staining and terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
42 vioral changes were associated with terminal deoxynucleotidyl transferase dUTP nick end labeling (TUN
43 l keratocytes (CD34), of apoptosis (terminal deoxynucleotidyl transferase dUTP nick end labeling [TUN
44 ssays) and resistance to apoptosis (terminal deoxynucleotidyl transferase dUTP nick end labeling and
45 ecombinants exhibited a decrease in terminal deoxynucleotidyl transferase dUTP nick end labeling and
46 o lung function and stereology, and terminal deoxynucleotidyl transferase dUTP nick end labeling assa
47 y lactate dehydrogenase release and terminal deoxynucleotidyl transferase dUTP nick end labeling of t
49 sed for viability and apoptosis via terminal deoxynucleotidyl transferase dUTP nick end labeling stai
51 ivity, chromatin fragmentation, and terminal deoxynucleotidyl transferase dUTP nick end labeling), an
52 5+/-4% versus 36+/-8%; P=0.004) and terminal deoxynucleotidyl transferase dUTP nick end labeling-posi
53 osis (caspase 3 activity and TUNEL [terminal deoxynucleotidyl transferase dUTP nick end labeling])-po
54 dehydrogenase leakage), apoptosis (terminal deoxynucleotidyl transferase dUTP nick end labelingc cel
55 ture of Bruch's membrane, there was terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUN
56 poptotic cells were identified with terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUN
58 1 month after MI, the frequency of terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUN
59 tion attenuated HIRI as measured by terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUN
63 ceptor degeneration was assessed by terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUN
64 able by cleaved caspase-3 staining, terminal deoxynucleotidyl transferase dUTP nick-end labeling assa
65 Hepatic apoptosis was detected by a terminal deoxynucleotidyl transferase dUTP nick-end labeling assa
66 pithelial apoptosis was assessed by terminal deoxynucleotidyl transferase dUTP nick-end labeling assa
67 membrane permeability and blebbing, terminal deoxynucleotidyl transferase dUTP nick-end labeling posi
68 le cells and endothelial cells were terminal deoxynucleotidyl transferase dUTP nick-end labeling posi
69 Caspase-3 cleavage/activity and terminal deoxynucleotidyl transferase dUTP nick-end labeling stai
71 serum alanine transaminase levels, terminal deoxynucleotidyl transferase dUTP nick-end labeling stai
72 -P2X(7) cells as ascertained by the terminal deoxynucleotidyl transferase dUTP nick-end labeling tech
73 ntage of cell death, as measured by terminal deoxynucleotidyl transferase dUTP nick-end labeling, was
74 r, there is a threefold increase in terminal deoxynucleotidyl transferase dUTP nick-end labeling-posi
75 pase-3 activation and appearance of terminal deoxynucleotidyl transferase dUTP nick-end labeling-posi
76 increase in caspase-3 activity and terminal deoxynucleotidyl transferase dUTP nick-end labeling-posi
77 xt day and analyzed by means of the terminal deoxynucleotidyl transferase dUTP-biotin nick-end-labeli
78 ye and retinas were analyzed by the terminal-deoxynucleotidyl transferase dUTP-linked nick end labeli
79 mistry, immunoblot analysis and the terminal-deoxynucleotidyl transferase dUTP-linked nick-end labeli
81 he decreased frequency of TUNEL(+) (terminal deoxynucleotidyl transferase mediated deoxyuridine triph
82 romo-deoxyuridine incorporation and terminal deoxynucleotidyl transferase mediated dUTP nick end labe
83 eling by propidium iodide staining; terminal deoxynucleotidyl transferase mediated dUTP nick end labe
84 nsities were measured with Ki67 and terminal deoxynucleotidyl transferase mediated dUTP nick end labe
85 se 3 activity and fluorescent-based terminal deoxynucleotidyl transferase mediated nick end labelling
88 anti-B7.2, or anti-CTLA4 and TUNEL (terminal deoxynucleotidyl transferase nick-end-labeling) analysis
89 caspase-3 immunohistochemistry, and terminal deoxynucleotidyl transferase UTP nick-end labeling (TUNE
90 is of heavily modified DNA, whereas terminal deoxynucleotidyl transferase was used for a single-nucle
91 receptor 7 alpha(+), c-kit(lo) and terminal deoxynucleotidyl transferase(+)) were selectively deplet
92 g laminin-5, MMPs, TGF beta, zyxin, terminal deoxynucleotidyl transferase, and angiogenesis-related p
93 dUTP nick end-labeling mediated by terminal deoxynucleotidyl transferase, associated with a robust i
94 olymerase mu (pol mu) is related to terminal deoxynucleotidyl transferase, but its biological role is
95 mplated (N) nucleotides inserted by terminal deoxynucleotidyl transferase, which resulted in a decrea
97 itive for cleaved caspase-3 and for terminal deoxynucleotidyl transferase-mediated biotin-dUTP nick-e
98 ng electron microscopy, and in situ terminal deoxynucleotidyl transferase-mediated biotin-dUTP nick-e
99 each parental genotype while TUNEL (terminal deoxynucleotidyl transferase-mediated biotinylated dUTP
100 osis were evidenced by increases in terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
101 abain injection, maximal numbers of terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
103 cord ventral horn were positive for terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
104 ity was assessed by O4 staining and terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
106 l growth factor receptor, a few are terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
109 Purkinje cell loss was analyzed by terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
110 d that deltaV1-1 reduced numbers of terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
111 brain areas developed infarcts and terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
112 from individual active caspase 3(+)/terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
113 ere was a 55.6% reduction in TUNEL (terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
114 NeuN)-immunoreactive cells are also terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
115 sed in neurons and colocalized with terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
120 s induced by KA were explored using terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
121 ces neuronal apoptosis, detected by terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
122 is little cell death, as assayed by terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
123 eavage product appeared at 48 hr in terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
125 ctivity for single-stranded DNA and terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
126 caspase-cleaved tau, but no TUNEL (terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
127 ined by active caspase-3 and TUNEL (terminal deoxynucleotidyl transferase-mediated biotinylated UTP n
128 ic effect of MT, as determined by a terminal deoxynucleotidyl transferase-mediated deoxyuridine 5-tri
129 aspase-9, and positive staining for terminal deoxynucleotidyl transferase-mediated deoxyuridine 5-tri
130 cytometry, electron microscopy, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
131 III immunocytochemical staining and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
132 sing bromodeoxyuridine staining and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
133 ma-counting, cleaved caspase-3, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
134 uantitated by nuclear morphology or terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
135 a 2-fold reduction in the number of terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
136 niques (hematoxylin-eosin staining, terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
137 , the expression of Fas ligand, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
138 5), bromodeoxyuridine (p<0.05), and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
139 istology, immunohistochemistry, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
140 At 2 wk, hematoxylin-eosin and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
141 degradation that can be detected by terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
142 tic necrosis and leads to pervasive terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
143 sitive cells, ganglion cells, and a terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
145 -activated cell sorter analysis and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
146 , DNA fragmentation, and apoptosis (terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
147 anol-induced apoptosis, assessed by terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
148 -2-phenylindole dihydrochloride and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
149 sensory-deprived rat olfactory bulb terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
150 hods: light microscopy, fluorescent terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
152 focal adhesion kinase and increased terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
153 stry, laser-capture microscopy, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
154 ed histone H3, activated caspase-3, terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
155 ed by Ki67 immunohistochemistry and terminal deoxynucleotidyl transferase-mediated deoxyuridine triph
157 on of apoptosis, assessed by TUNEL (terminal deoxynucleotidyl transferase-mediated dNTP-biotin nick e
158 und at 4 h by DNA fragmentation and terminal deoxynucleotidyl transferase-mediated dUPT nick-end labe
159 ial cells (BAECs), as determined by terminal deoxynucleotidyl transferase-mediated dUTP biotin nick-e
160 , 6-diamino-2-phenylindole), TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick and labe
161 e cleavage, Annexin V staining, and terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
162 taining for Ki-67 and cyclin D1 and terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
164 , cardiac apoptosis was examined by terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
165 sed intratumoral apoptotic index by terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
166 o)benzene sulfonic acid) and TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
167 tosis indicated by nuclear changes, terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
169 sis was measured by flow cytometry, terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
170 n of piriform cortex, on apoptosis (terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
171 dol and reduced haloperidol induced terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
172 observed with the use of either the terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
173 ld type protein had very low TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
174 ase, ii) DNA ladder formation, iii) terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
175 t resulted in a marked reduction in terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
176 in-dATP nick translation (PANT) and terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
177 on cells as assessed by morphology, terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
178 stration resulted in an increase in terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
179 ings its expression correlated with terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
180 ld) and HA expression but increased terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
181 of apoptosis, as measured by TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
182 nificantly increased the percent of terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
183 ADP-ribose) polymerase cleavage and terminal deoxynucleotidyl transferase-mediated dUTP nick end labe
184 frequency of intrahepatic apoptotic terminal deoxynucleotidyl transferase-mediated dUTP nick end-labe
185 alyzed for apoptotic nuclei using a terminal deoxynucleotidyl transferase-mediated dUTP nick end-labe
186 caspase-activated DNase levels, and terminal deoxynucleotidyl transferase-mediated dUTP nick end-labe
187 omo-2'-dUTP incorporation assay and terminal deoxynucleotidyl transferase-mediated dUTP nick end-labe
191 rons in heart failure, we performed terminal deoxynucleotidyl transferase-mediated dUTP nick end-labe
192 occludin, Ki-67, NF-kappaB-p65, and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
193 l apoptotic cells in Drosophila are terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
194 e uptake, and apoptotic cell death (terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
195 ologic damage, cytokine expression, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
196 s in the diaphragm (e.g., number of terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
197 ptosis was assessed with the use of terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
198 y, as well as apoptosis detected by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
199 ion of apoptosis as revealed by the terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
200 s within the retina was examined by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
202 nstrated by positive staining using terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
203 less apoptosis as measured by both terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
205 scent staining, and flow-cytometric terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
206 analysis, immunocytochemistry, and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
207 [BrdU]) and cell death (caspase-3, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
208 8-72 h, marked by nuclear blebbing, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
209 cell death occurred as detected by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
210 on factor 2 alpha), and cell death [terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
211 area that also showed more positive terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
214 by hematoxylin and eosin staining, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
215 eocytes/periosteal osteoblasts with terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
216 size, reduced Ki-67, and increased terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
217 helial markers CD31 and VEGFR-2 and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
218 AR(-/-) mice had significantly more terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
220 e by Western blot, and apoptosis by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
222 orneas, whereas it colocalized with terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
223 chamber assay), and antiapoptotic (terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
224 the culture plate over time, became terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
225 cription polymerase chain reaction, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
226 nsferase (ALT), caspase-3 activity, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
227 ly, the number of diabetes-enhanced terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
228 se-induced apoptosis as measured by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
229 and less contraction band necrosis, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
230 ice displayed a 13-fold increase in terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
231 -increased activated caspase-3- and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labe
234 entation, measured by the number of terminal deoxynucleotidyl transferase-mediated dUTP nick-end-labe
235 Apoptosis was assessed by using terminal deoxynucleotidyl transferase-mediated dUTP-biotin end la
236 aused DNA degradation as evident by terminal deoxynucleotidyl transferase-mediated dUTP-biotin end la
237 LX-2 cells, as was confirmed by the terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick e
238 ate dehydrogenase release assay and terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick e
239 caspases 3 and 8, and the number of terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick e
240 n vitro at 72 hours (P < 0.05), and terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick e
243 ell death were investigated by MTT, terminal deoxynucleotidyl transferase-mediated dUTP-digoxigenin n
244 ned, and evaluated for apoptosis by terminal deoxynucleotidyl transferase-mediated dUTP-digoxigenin n
245 tive (Ac)-caspase-3, -8, and -9 and terminal deoxynucleotidyl transferase-mediated dUTP-digoxigenin n
246 termined by Hoechst 33342 staining, terminal deoxynucleotidyl transferase-mediated dUTP-FITC nick end
247 ained for interleukin (IL)-12 or by terminal deoxynucleotidyl transferase-mediated dUTP-nick end labe
249 ted levels of apoptosis observed by terminal deoxynucleotidyl transferase-mediated nick end labeling
250 indicated by caspase-3 activity and terminal deoxynucleotidyl transferase-mediated nick end labeling
251 using flow cytometric Annexin V and terminal deoxynucleotidyl transferase-mediated nick end labeling
252 t did not involve apoptosis because terminal deoxynucleotidyl transferase-mediated nick end labeling
254 revealed by caspase activation and terminal deoxynucleotidyl transferase-mediated nick end labeling
255 rouracil (5-FU), induced apoptosis (terminal deoxynucleotidyl transferase-mediated nick end labeling
256 cells were apoptotic as judged by a terminal deoxynucleotidyl transferase-mediated nick end labeling
260 atine kinase release) or apoptosis (terminal deoxynucleotidyl transferase-mediated nick end labeling
261 and apoptosis was evaluated by the terminal deoxynucleotidyl transferase-mediated nick end labeling
262 OX-42, gamma-aminobutyric acid, or terminal deoxynucleotidyl transferase-mediated nick end labeling
263 s as measured by flow cytometry and terminal deoxynucleotidyl transferase-mediated nick end labeling
264 histochemical double labeling with terminal deoxynucleotidyl transferase-mediated nick end labeling
265 ors were apoptotic as determined by terminal deoxynucleotidyl transferase-mediated nick end labeling
266 and protected against diabetes, and terminal deoxynucleotidyl transferase-mediated nick end labeling
267 d tumor cell apoptosis (assessed by terminal deoxynucleotidyl transferase-mediated nick end labeling)
268 SK-RC-45 line stimulated the TUNEL (terminal deoxynucleotidyl transferase-mediated nick end labeling)
269 luorescence-activated cell sorting, terminal deoxynucleotidyl transferase-mediated nick end labeling,
272 tion, and a significant increase in terminal deoxynucleotidyl transferase-mediated nick end labeling-
273 mitochondria to the cytoplasm, and terminal deoxynucleotidyl transferase-mediated nick end labeling.
275 s was also noted in PiZ BDL mice by terminal deoxynucleotidyl transferase-mediated nick-end labeling
276 re employed in cells resistant (<5% terminal deoxynucleotidyl transferase-mediated nick-end labeling
277 notransferase (ALT), pathology, and terminal deoxynucleotidyl transferase-mediated nick-end labeling
278 in the apoptosis rate was observed (terminal deoxynucleotidyl transferase-mediated nick-end labeling
280 arvested and assayed for apoptosis (terminal deoxynucleotidyl transferase-mediated nick-end labeling)
281 s, as shown by increased numbers of terminal deoxynucleotidyl transferase-mediated nick-end labeling-
282 DNA fragmentation was evaluated by terminal deoxynucleotidyl transferase-mediated uridine 5'-triphos
283 tochrome c immunohistochemistry and terminal deoxynucleotidyl transferase-mediated uridine 5'-triphos
284 Neuronal cell death was examined by terminal deoxynucleotidyl transferase-mediated uridine 5'-triphos
285 was observed with the appearance of terminal deoxynucleotidyl transferase-mediated UTP end labeling r
286 hematoxylin and eosin-stained, and terminal deoxynucleotidyl transferase-mediated UTP nick end-label
287 expression was induced primarily in terminal deoxynucleotidyl transferase-mediated UTP nick-end label
293 Apoptosis was determined by the terminal deoxynucleotidyl- transferase-dUTP nick-end labeling ass
294 Apoptosis was evaluated by in situ terminal deoxynucleotidyl-transferase mediated dUTP nick end labe
295 findings, flow cytometry and TUNEL (terminal deoxynucleotidyl-transferase-mediated dUTP nick end labe
296 were studied by routine microscopy, terminal deoxynucleotidyl-transferase-mediated dUTP nick-end labe
297 endothelial cells as determined by terminal deoxynucleotidyl-transferase-mediated dUTP nick-end labe
299 liferating cell nuclear antigen and terminal deoxynucleotidyl-transferase-mediated dUTP nick-end stai
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